TY - JOUR
T1 - Phase-Transformable DNA Frameworks for Synthetic Condensates with Valency-Controlled Subcellular Sorting
AU - Yu, Haozhen
AU - Zhao, Ziyi
AU - Lv, Haoyue
AU - Xu, Zhiqian
AU - Han, Zhaoyu
AU - Liu, Biwu
AU - Zhao, Yongxi
N1 - Publisher Copyright:
© 2026 American Chemical Society
PY - 2026/6/17
Y1 - 2026/6/17
N2 - Synthetic control of intracellular phase separation offers exciting opportunities for engineering artificial membraneless organelles (MLOs). However, achieving precise control of DNA-based condensates in complex cellular environments remains challenging. Here, we present a phase-transforming DNA framework that enables the in situ transition of tetrahedral DNA nanostructures into functional condensates through valency-controlled subcellular sorting. With coarse-grained simulations and experiments, we demonstrate that the condensation order is governed by binding valencies of transformed building blocks. Strikingly, we revealed distinct intracellular fates of synDNA condensates, with high-order condensates escaping the endolysosomal pathway and low-order condensates trapped in the lysosome. Furthermore, we demonstrate that spatially controlled DNA condensates serve as versatile artificial MLOs, facilitating the targeted degradation of membrane proteins and prolonging the cytosolic residence of the therapeutic payloads. Our findings establish a modular design principle for constructing programmable DNA condensates in cellulo, underscoring the profound interactions between synthetic biological constructs and cellular organelles.
AB - Synthetic control of intracellular phase separation offers exciting opportunities for engineering artificial membraneless organelles (MLOs). However, achieving precise control of DNA-based condensates in complex cellular environments remains challenging. Here, we present a phase-transforming DNA framework that enables the in situ transition of tetrahedral DNA nanostructures into functional condensates through valency-controlled subcellular sorting. With coarse-grained simulations and experiments, we demonstrate that the condensation order is governed by binding valencies of transformed building blocks. Strikingly, we revealed distinct intracellular fates of synDNA condensates, with high-order condensates escaping the endolysosomal pathway and low-order condensates trapped in the lysosome. Furthermore, we demonstrate that spatially controlled DNA condensates serve as versatile artificial MLOs, facilitating the targeted degradation of membrane proteins and prolonging the cytosolic residence of the therapeutic payloads. Our findings establish a modular design principle for constructing programmable DNA condensates in cellulo, underscoring the profound interactions between synthetic biological constructs and cellular organelles.
UR - https://www.scopus.com/pages/publications/105042146389
U2 - 10.1021/jacs.6c04988
DO - 10.1021/jacs.6c04988
M3 - 文章
C2 - 42231671
AN - SCOPUS:105042146389
SN - 0002-7863
VL - 148
SP - 24184
EP - 24197
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 23
ER -